RETAINE HPMC (hypromellose 2910- 4000 mpa.s solution/ drops

retaine HPMC by

Drug Labeling and Warnings

retaine HPMC by is a Otc medication manufactured, distributed, or labeled by OCuSOFT, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient Hypromellose 0.3%

Purpose Eye lubricant

Uses  ▪ For the temporary releif of burning, irritation and discomfort due to dryness of the eye, or exposure to wind or sun. ▪ May be used as a protectant against further ittitation.

Warnings
▪ For use in the eyes only. 

Do not use if solution changes color or becomes cloudy.

When using this product
 ▪ do not touch tip of container to any surface to avoid contamination.
 ▪ replace cap after use.

Stop use and ask a doctor if ▪ you experience eye pain, changes in vision, continued redness or irritation of the eye. ▪ the condition worsens or persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

▪ Instill 1 or 2 drops in the affected eye(s) as needed.

Other Information

▪ Use only it tamper seals on top ad bottom flaps are intact.
▪ Store between 15°-30°C (59°-86°F).
▪ Keep carton for complete product information.  
▪ Discard after 12 weeks.

Inactive ingredients

Citric acid, sodium citrate, sorbitol, water for injection.

Questions?

☏(800)233-5469 M-F
8:30AM-5:00PM CST
www.retainebrand.com

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INGREDIENTS AND APPEARANCE

RETAINE HPMC 
hypromellose 2910 (4000 mpa.s) solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54799-896
Route of Administration	OPHTHALMIC, TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Hypromellose 2910 (4000 Mpa.s) (UNII: RN3152OP35) (Hypromellose 2910 (4000 Mpa.s) - UNII:RN3152OP35)	Hypromellose 2910 (4000 Mpa.s)	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Anhydrous Citric Acid (UNII: XF417D3PSL)
Sodium Citrate (UNII: 1Q73Q2JULR)
Sorbitol (UNII: 506T60A25R)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54799-896-10	10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/01/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	05/01/2013

Labeler - OCuSOFT, Inc. (174939207)

Registrant - OCuSOFT, Inc. (174939207)